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rs1064794069

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position67722826
GeneAR
is asnp
is mentioned by
dbSNPrs1064794069
dbSNP (old)rs1064794069
ClinGenrs1064794069
ebirs1064794069
HLIrs1064794069
Exacrs1064794069
Gnomadrs1064794069
Varsomers1064794069
Maprs1064794069
PheGenIrs1064794069
Biobankrs1064794069
1000 genomesrs1064794069
hgdprs1064794069
ensemblrs1064794069
gopubmedrs1064794069
geneviewrs1064794069
scholarrs1064794069
googlers1064794069
pharmgkbrs1064794069
gwascentralrs1064794069
openSNPrs1064794069
23andMers1064794069
23andMe allrs1064794069
SNPshotrs1064794069
SNPdbers1064794069
MSV3drs1064794069
GWAS Ctlgrs1064794069
Max Magnitude0
ClinVar
Risk rs1064794069(A;A)
Alt rs1064794069(A;A)
Reference Rs1064794069(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene AR
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.66942668G>A
CLNSRC
CLNACC RCV000482716.1,